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Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes

Blastocystis is a unicellular stramenopile of controversial pathogenicity in humans [1, 2]. Although it is a strict anaerobe, Blastocystis has mitochondrion-like organelles with cristae, a transmembrane potential and DNA [2–4]. An apparent lack of several typical mitochondrial pathways has led some...

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Autores principales: Stechmann, Alexandra, Hamblin, Karleigh, Pérez-Brocal, Vicente, Gaston, Daniel, Richmond, Gregory S., van der Giezen, Mark, Clark, C. Graham, Roger, Andrew J.
Formato: Texto
Lenguaje:English
Publicado: Cell Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2428068/
https://www.ncbi.nlm.nih.gov/pubmed/18403202
http://dx.doi.org/10.1016/j.cub.2008.03.037
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author Stechmann, Alexandra
Hamblin, Karleigh
Pérez-Brocal, Vicente
Gaston, Daniel
Richmond, Gregory S.
van der Giezen, Mark
Clark, C. Graham
Roger, Andrew J.
author_facet Stechmann, Alexandra
Hamblin, Karleigh
Pérez-Brocal, Vicente
Gaston, Daniel
Richmond, Gregory S.
van der Giezen, Mark
Clark, C. Graham
Roger, Andrew J.
author_sort Stechmann, Alexandra
collection PubMed
description Blastocystis is a unicellular stramenopile of controversial pathogenicity in humans [1, 2]. Although it is a strict anaerobe, Blastocystis has mitochondrion-like organelles with cristae, a transmembrane potential and DNA [2–4]. An apparent lack of several typical mitochondrial pathways has led some to suggest that these organelles might be hydrogenosomes, anaerobic organelles related to mitochondria [5, 6]. We generated 12,767 expressed sequence tags (ESTs) from Blastocystis and identified 115 clusters that encode putative mitochondrial and hydrogenosomal proteins. Among these is the canonical hydrogenosomal protein iron-only [FeFe] hydrogenase that we show localizes to the organelles. The organelles also have mitochondrial characteristics, including pathways for amino acid metabolism, iron-sulfur cluster biogenesis, and an incomplete tricarboxylic acid cycle as well as a mitochondrial genome. Although complexes I and II of the electron transport chain (ETC) are present, we found no evidence for complexes III and IV or F(1)F(o) ATPases. The Blastocystis organelles have metabolic properties of aerobic and anaerobic mitochondria and of hydrogenosomes [7, 8]. They are convergently similar to organelles recently described in the unrelated ciliate Nyctotherus ovalis[9]. These findings blur the boundaries between mitochondria, hydrogenosomes, and mitosomes, as currently defined, underscoring the disparate selective forces that shape these organelles in eukaryotes.
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spelling pubmed-24280682008-06-13 Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes Stechmann, Alexandra Hamblin, Karleigh Pérez-Brocal, Vicente Gaston, Daniel Richmond, Gregory S. van der Giezen, Mark Clark, C. Graham Roger, Andrew J. Curr Biol Report Blastocystis is a unicellular stramenopile of controversial pathogenicity in humans [1, 2]. Although it is a strict anaerobe, Blastocystis has mitochondrion-like organelles with cristae, a transmembrane potential and DNA [2–4]. An apparent lack of several typical mitochondrial pathways has led some to suggest that these organelles might be hydrogenosomes, anaerobic organelles related to mitochondria [5, 6]. We generated 12,767 expressed sequence tags (ESTs) from Blastocystis and identified 115 clusters that encode putative mitochondrial and hydrogenosomal proteins. Among these is the canonical hydrogenosomal protein iron-only [FeFe] hydrogenase that we show localizes to the organelles. The organelles also have mitochondrial characteristics, including pathways for amino acid metabolism, iron-sulfur cluster biogenesis, and an incomplete tricarboxylic acid cycle as well as a mitochondrial genome. Although complexes I and II of the electron transport chain (ETC) are present, we found no evidence for complexes III and IV or F(1)F(o) ATPases. The Blastocystis organelles have metabolic properties of aerobic and anaerobic mitochondria and of hydrogenosomes [7, 8]. They are convergently similar to organelles recently described in the unrelated ciliate Nyctotherus ovalis[9]. These findings blur the boundaries between mitochondria, hydrogenosomes, and mitosomes, as currently defined, underscoring the disparate selective forces that shape these organelles in eukaryotes. Cell Press 2008-04-22 /pmc/articles/PMC2428068/ /pubmed/18403202 http://dx.doi.org/10.1016/j.cub.2008.03.037 Text en © 2008 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Report
Stechmann, Alexandra
Hamblin, Karleigh
Pérez-Brocal, Vicente
Gaston, Daniel
Richmond, Gregory S.
van der Giezen, Mark
Clark, C. Graham
Roger, Andrew J.
Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes
title Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes
title_full Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes
title_fullStr Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes
title_full_unstemmed Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes
title_short Organelles in Blastocystis that Blur the Distinction between Mitochondria and Hydrogenosomes
title_sort organelles in blastocystis that blur the distinction between mitochondria and hydrogenosomes
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2428068/
https://www.ncbi.nlm.nih.gov/pubmed/18403202
http://dx.doi.org/10.1016/j.cub.2008.03.037
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